List of variants in gene TYR reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.1366+4A>G	rs61754398	0.00175
NM_000372.5(TYR):c.915C>A (p.Asp305Glu)	rs142170797	0.00017
NM_000372.5(TYR):c.1046G>C (p.Ser349Thr)	rs1010038586	0.00002
NM_000372.5(TYR):c.1213C>T (p.Arg405Cys)	rs746811736	0.00002
NM_000372.5(TYR):c.864A>T (p.Leu288Phe)	rs371985121	0.00001
NM_000372.5(TYR):c.1501C>T (p.Arg501Cys)
NM_000372.5(TYR):c.1588T>A (p.Ter530Lys)	rs2135332829
NM_000372.5(TYR):c.391_393del (p.Lys131del)	rs1413017181
NM_000372.5(TYR):c.755T>G (p.Met252Arg)	rs1943262190

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